Upload
others
View
5
Download
0
Embed Size (px)
Citation preview
Electronic Supplementary Information (ESI) for Journal of Materials
Chemistry A
High-Efficiency Non-Halogenated Solvent Processable Polymer/PCBM Solar Cells via Fluorination-Enabled Optimized Nanoscale Morphology
Shafket Rasool,†ab Quoc Viet Hoang,†a Doan Van Vu,†a Thi Thu Trang Bui,c
Seon-Mi Jin,d Thuy Thi Ho,ab Chang Eun Song,*ab Hang Ken Lee,a Sang Kyu
Lee,ab Jong-Cheol Lee,ab Sang-Jin Moon,ab Eunji Lee,*e and Won Suk Shin*abf
aEnergy Materials Research Center, Korea Research Institute of Chemical Technology (KRICT),
141 Gajeongro, Yuseong, Daejeon 34114, Republic of Korea. E-mail: [email protected],
bAdvanced Materials and Chemical Engineering, University of Science and Technology (UST),
217 Gajeongro, Yuseong, Daejeon 34113, Republic of Korea.
cDepartment of Chemical Technology, Hanoi University of Industry (HaUI), No. 298 Cau Dien
Street, Bac Tu Liem District, Hanoi, Vietnam
dGraduate School of Analytical Science and Technology, Chungnam National University, 99 Daehakro,
Yuseong, Daejeon 34134, Republic of Korea.
eSchool of Materials Science and Engineering, Gwangju Institute of Science and Technology
(GIST), 123 Cheomdangwagiro, Bukgu, Gwangju, 61005, Republic of Korea. E-mail:
Electronic Supplementary Material (ESI) for Journal of Materials Chemistry A.This journal is © The Royal Society of Chemistry 2019
fKU-KRICT Collaborative Research Center & Division of Display and Semiconductor Physics &
Department of Advanced Materials Chemistry, Korea University, 2511 Sejong-ro, Sejong
30019, Republic of Korea.
†First authors
S.R., Q.V.H. and D.V.V. contributed equally to this work.
*Corresponding Author
C.E.S.: [email protected], E.L.: [email protected] and W.S.S.: [email protected]
Experimental Section
Nuclear magnetic resonance (NMR): 1H NMR spectrum was recorded on Bruker AVANCE 400
MHz spectrometer.
UV-vis absorption: UV-vis absorption spectra were recorded using Shimadzu UV-36000
spectrophotometer with solution in chloroform and thin film on quartz substrate.
Thermogravimetric (TGA): TGA measurements were carried out on Thermo plus EVOII TG8120
under nitrogen flow with a heating rate of 10 oC min-1.
Differential scanning calorimetry (DSC): DSC measurements were performed on
Thermogravimetric analyzer (Model Q-1000) under nitrogen with heating rate of 10 oC min-1.
Cylic voltammetry (CV): Electrochemical measurements were performed under argon
atmosphere with tetra-n-butylammonium hexafluorophosphate (0.1 M) in anhydrous
acetonitrile using IVIUMSTAT instrument model PV-08 at a scan rate of 20 mV s-1. Polymers
were coated on platinum working electrode, platinum-wire using as counter electrode and
Ag/AgNO3 using as reference electrode. The potentials were calibrated with
ferrocene/ferrocenium, which is located at -4.8 eV respect to vacuum level.
Atomic Force Microscopy (AFM): AFM specimens were prepared by using the same procedures
with optimal conditions but without MoO3/Ag top electrode.
Transition Electron Microscopy (TEM): TEM samples were prepared casting the blend film with
optimum condition on ITO/PEDOT:PSS substrate , then floating the film on water surface, and
transferring into TEM grids. The TEM images were taken on JEOL JEM-2200FS.
Device Fabrication and Measurement: Inverted device architecture Glass/ITO/ZnO
NPs/PEIE/photoactive layer/MoO3/Ag is used for the fabrication of fullerene-based PSCs. Strip
patterned ITO-glass with sheet resistance of 15Ω sq-1 is used as a substrate. First of all, The
ITO-glass substrate was washed three times with deionized water with few drops of cleaning
detergent, followed by washing three times each in acetone and IPA. After drying in hot oven
at 140 oC overnight, these substrates were treated with UVO for 15 minutes. ZnO NPs (nano
clean tech.) was spin coated over ITO-glass substrate at 3000 rpm for 30 seconds and then
annealed at 100 oC for 10 minutes to get a compact electron transport layer (ETL) wtih 35 nm
thickness. Ethoxylated polyethylenimine solution (PEIE) was spin coated (0.2 wt% in 2-methoxy
ethanol) over ZnO ETL at 5000 rpm for 30 seconds and then annealed at 100 oC for 10
minutes. Polymer:PC71BM (1:1.5, w/w) blend solutions were prepared in o-xylene (xyl) solvent
with and without 3 vol% diphenyl ether (DPE) with the concentration of 2.35 wt% for
polymer:PC71BM. Solutions were stirred overnight at 70 oC and at 110 oC for 3 hours before
filtration by using 5um PTFE filter. Photoactive layers have been spin coated from hot solutions
(110 oC) over hot substrates (100 oC) at 800 rpm to get the optimized thicknesses, according
to already reported procedure. After three hours of drying the photoactive layers in the glove
box, the substrates were transferred to metal deposition chamber where 10 nm of MoO3 and
100 nm of Ag was thermally evaporated under the vacuum of nearly 10-7 mbar. 0.09 cm2
shadow mask is used to measure PCE. Keithley 2400 source meter and solar simulator (K201
LAB55, McScience) is used for PCE measurement while K3100 IQX, McScience is used to
measure external quantum efficiency. Before PCE measurement, the solar simulator intensity
was calibrated using NREL certified silicon diode with an integrated KG1 optical filter. The
current densities obtained from solar simulator were compared with the integrated current
densities from the EQE.
Charge Carrier Mobilities: For hole-only devices, following architecture is used:
Glass/ITO/PEDOT:PSS (30nm)/photoactive layer/Au (100nm), while for electron-only devices,
following architecture is used: Glass/ITO/ZnO NPs(30nm)/PEIE/Photoactive
layer/Ca(2nm)/Al(100nm). For hole-mobilities for neat polymers, 1.5wt% solution of each
polymer was prepared in o-xylene solvent while for blend films, similar conditions (as
described in the earlier section for blend solutions) have been used. PEDOT:PSS (AI4083,
HERAUS) was spin coated on the ITO substrate at 5000 rpm to get nearly 30 nm film and
then annealed in air at 150 oC for 30 min. After coating photoactive layers in the N2-filled
glove box, devices were completed by depositing 100 nm of Au. For electron-only devices,
after coating ZnO NPs (30 nm)/PEIE ETL on the ITO substrate, photoactive layers were coated
and the devices were completed by depositing 2 nm of Ca and 100 nm of Al. Devices were
encapsulated with glass using UV-curable resin, followed by measuring the single carrier
charge mobility in dark from the space-charge limited current (SCLC) region.
2D-GIWAXS: ZnO NPs/PEIE ETL was coated over the silicon substrate followed by the coating
of the photoactive layer under optimized conditions. Beamline PLS-II 3C was used at Pohang
Accelerator Laboratory (PAL) in Republic of Korea. ~2 min was given to the X-ray irradiation
to reach the saturation level and the incident angle of 0.11~0.14o was selected for the incident
X-rays to penetrate enough in the photoactive film to obtain a clear 2D-GIWAXS image.
NEXAFS: Beamline PES 4D was used at Pohang Accelerator Laboratory (PAL) in Republic of
Korea. NEXAFS spectra were recorded in the total electron yield (TEY) mode by measuring the
sample current normalized to signal current; simultaneously measured using a gold mesh in
10-9 torr vacuum. A fourfold symmetry of the substrate was used with photon beam to
determine the tilt angle (α) between the C=C double bond in the conjugated planes and the
Si substrate surface. Average chain conformation of the polymer films have been determined
by calculating the dichroic (R) ratios using the formula:
𝑅 = 𝐼(90°) ‒ 𝐼(0°)𝐼(90°) + 𝐼(0°)
Where R is the difference between the intensities at θ= 90o and 0o, divided by their sum.
Transmission Electron Microscopy Tomography (TEMT): Photoactive films were spin coated
using the same method for preparation of TEM samples as described above. JEM-1400 (JEOL,
Japan) is used for the TEMT analysis. TEM images at different tilting angles after each tilting,
refocusing and repositioning have been recorded using Veleta or Tengra CCD camera. IMOD
software used for alignment and reconstruction of the tilt series, while Amira visualization
software from FEI has been utilized for 3D-visualizations and quantitative volumetric analysis
of the polymer:PC71BM blend films under optimum conditions.
Material Syntheses
All chemicals and solvents were purchased from Aldrich, Alfa Aesar and TCI Chemical Co. All
solvents have been purchased from sigma aldrich, unless otherwise specified. Monomer 8
(5,5’-bis(trimethylstannyl)-3-fluoro-2,2’-bithiophene ) has been synthesized using the following
(below) procedure while 5,5’-bis(trimethylstannyl)-3,3’-difluoro-2,2’-bithiophene have been
synthesized using the procedures as mentioned in the literature.S1 5,10-bis(5-bromo-4-(2-
decyltetradecyl)thiophen-2-yl)naphtho[1,2-c:5,6-c']bis([1,2,5]thiadiazole) was synthesized
according to the literatures with modification.S2
Syntheses of Monomer
S
S
S
S
Br
BrBr
NBS
CF/AcOH
1 2
3,5,5’-tribromo-2,2’-bithiophene (2): 2,2’-bithiophene (5.00 g, 30.07 mmol) and N-
bromosuccinimide (16.13 g, 90.60 mmol) were dissolved in 150 mL mixture of
chloroform/AcOH (3:2, v/v). The reaction mixture was refluxed at 60 oC for 6h under argon
protection. Then, mixture of water and chloroform was added and the reaction mixture was
stirred for 30 mins. The organic layer was extracted and dried over magnesium sulfate
anhydrous and filtered. The organic solvent was removed under reduced pressure to obtain
gray solid. The residue was washed with hexane and then recrystallized with mixture of
chloroform and methanol to afford desired compound 2 (9.81 g, 24.36 mmol) with yield of
81%. 1H NMR (400 MHz, CDCl3): δ (ppm) 7.05 (1H, d, J= 4 Hz), 7.01 (1H, d, J= 4 Hz), 6.89 (1H,
s). 13C NMR (400 MHz, CDCl3): δ (ppm) 133.7; 132.7; 132.1; 129.0; 126.0; 112.7; 110.5; 106.3.
MS (EI): Calcd, 402; found [M+1]+ 403.
S
S
Br
BrBr
S
SBr
Me3Si
SiMe3
1. n-BuLi
2. Me3SiCl
2 3
3-bromo-5,5’-bis(trimethylsilyl)-2,2’-bithiophene (3): Under argon atmosphere, 3,5,5’-
tribromo-2,2’-bithiophene 2 (6.00 g, 14.89 mmol) was dissolved in 100 mL of anhydrous THF.
The solution was cooled down to -78 oC, then 1.6 M n-BuLi in hexane (19.08 mL, 30.52 mmol)
was added slowly within 10 min. The reaction mixture was continued to stir at this temperature
for 1 hour, then gradually warmed to room temperature and stirred for 1 hour further. After
cooling again to -78 oC, trimethylsilyl choride (3.90 mL, 30.67 mmol) was added in one portion.
The reaction mixture was gradually warmed to room temperature and stirred overnight. The
reaction residue was quenched by 50 mL of water, then extracted two times with hexane to
obtain organic layer. The organic phase was dried over magnesium sulfate anhydrous,
concentrated under reduced pressure. The crude product was purified by silica column
chromatography with hexane as eluent to give desired product as light yellow oil 3 (4.70 g,
12.06 mmol) with yield of 81%. 1H NMR (400 MHz, CDCl3): δ (ppm) 7.52 (1H, d, J= 4 Hz), 7.21
(1H, d, J= 4 Hz), 7.11 (1H, s), 0.36 (9H, s), 0.34 (9H, s). 13C NMR (400 MHz, CDCl3): δ (ppm)
141.8; 140.0; 139.9; 138.5; 137.4; 134.6; 128.0; 109.1. MS (EI): Calcd, 388; found [M+2]+ 390.
S
SBr
Me3Si
SiMe3
1. n-BuLi
2. NFSI
S
SF
Me3Si
SiMe3
3 4
3-fluoro-5,5’-bis(trimethylsilyl)-2,2’-bithiophene (4): Under argon protection, 3-bromo-5,5’-
bis(trimethylsilyl)-2,2’-bithiophene 3 (4.70 g, 12.06 mmol) was dissolved in 100mL of
anhydrous THF. The solution was cooled down to -78 oC, then 1.6 M n-BuLi in hexane (8.30
mL, 13.27 mmol) was added slowly within 10 min. the reaction mixture was continued to
stirred at this temperature for 2 hours. N-Fluorobenzenesulfonimide (5.57 g, 14.47 mmol) was
dissolved in 20 mL of anhydrous THF and then was transferred to reaction mixture. The mixture
was gradually warmed to room temperature and stirred overnight. The reaction mixture was
quenched by water, extracted two times with hexanes. The combined organic layer was dried
over magnesium sulfate anhydrous, removed solvent under reduced pressure. The crude
product was loaded on silica column chromatography with hexane as eluent to obtain 3.09 g
of yellow oil 4 (3-fluoro-5,5’-bis(trimethylsilyl)-2,2’-bithiophene was major (95%) and small
impurities 5,5’-bis(trimethylsilyl)-2,2’-bithiophene were observed, which could not purify by
silica gel column).
S
S SiMe3F
S
SF
Me3Si
SiMe3
K2CO3
THF:MeOH
4 6
3-fluoro-5’-trimethylsilyl-2,2’-bithiophene (6): In round bottom flask, 3-fluoro-5,5’-
bis(trimethylsilyl)-2,2’-bithiophene 4 with small impurities (3.09 g) was dissolved in 150 mL
mixture of THF and MeOH (3:2, v/v). Anhydrous potassium carbonate (2.54 g, 18.35 mmol)
was added, then the reaction mixture was continued to stir at room temperature for 8h. Then,
100 mL of water was added to dissolve the excessive amount of potassium carbonate, then
extracted with hexane to obtain organic layer. The residue was dried over magnesium sulfate
anhydrous, concentrated under reduced pressure. The crude product was loaded on silica
column chromatography with hexane as eluent to obtain yellow oil 6 (1.74 g, 6.78 mmol) with
overall yield of 76%.
S
S SiMe3F
S
SF
(C4H9)4NF
6 7
3-Fluoro-2,2’-bithiophene (7): Tetrabutylammonium fluoride solution 1M in THF (15 mmol,
15 mL) was added to 3-fluoro-5’-(trimethylsilyl)-2,2’-bithiophene 6 (2.9 g, 11.3 mmol) solution
in THF (100 mL) at room temperature. After 1 hour, the reaction mixture was quenched with
water and extracted with diethyl ether. The organic phase was dried over anhydrous Na2SO4
and then concentrated by rotary evaporator. The crude product was purified by silica gel
column with hexanes as eluent to yield compound 7 as white solid (1.85 g, 89% yield). 1H
NMR (400 MHz, CDCl3): δ (ppm) 7.28 (1H, dd, J1= 5.2, J2= 1.1); 7.23 (1H, dd, J1= 3.6, J2= 1.1);
7.05 (2H, m); 6.84 (1H, d, J= 5.6). 19F NMR (470 MHz, CDCl3): δ (ppm) -129.56. MS (EI): Calcd,
184.0; found M+ 184.
S
SF
1. LDA
2. Me3SnCl
S
SF
Me3Sn
SnMe3
7 8
5,5’-Bis(trimethylstannyl)-3-fluoro-2,2’-bithiophene (8): 3-Fluoro-2,2’-bithiophene (1.85 g,
10.0 mmol) was dissolved in 100 mL of anhydrous THF under Argon atmosphere. The solution
was cooled down to −78 °C by a dry ice–acetone bath, and 2 M LDA solution (10.5 mL, 21
mmol) was added dropwise for 10 minutes. The reaction mixture was stirred at this
temperature for 1h and then trimethyl tin chloride solution (22 mL, 22 mmol, 1M in THF) was
added rapidly. The mixture was allowed to warm to room temperature and stirred overnight.
The reaction was quenched with 20 mL of NH4Cl solution and extracted with diethyl ether.
The organic extraction was washed by water twice and then dried over anhydrous Na2SO4.
After removing the solvent under vacuum, recrystallization of the residue from methanol
yielded monomer 8 (3.1 g, 61%) as colorless crystals. 1H NMR (400 MHz, CDCl3): δ (ppm) 7.32
(1H, d, J= 3.3); 7.11 (1H, d, J= 3.4); 6.88 (1H, d, J= 1.3); 0.38 (18H, m). 19F NMR (470 MHz,
CDCl3): δ (ppm) -131.24. MS (EI): Calcd, 509.9; found M+ 510.
Syntheses of Polymers
SBr
NS
N
NS
NC12H25
C10H21
SBr
C12H25C10H21
S SMe3Sn SnMe3+
S
NS
N
NS
NC12H25
C10H21
S
C12H25C10H21
S S
n
Pd2(dba)3 2%,P(o-Tol)3 8%
MW: 120 oC 10 mins150 oC 70 mins
PNTz4T
PNTz4T: 5,10-Bis(5-bromo-4-(2-decyltetradecyl)thiophen-2-yl)naphtho[1,2-c:5,6-
c′]bis[1,2,5]thiadiazole (124 mg, 0.10 mmol) and 5,5’-bis(trimethylstannyl)-2,2’-bithiophene (49
mg, 0.10 mmol) were added into a 5 mL microwave tube. Pd2(dba)3 (1.8 mg, 2 μmol) and
P(o-Tol)3 (2.4 mg, 8 μmol) were charged in the glove box. After capping, anhydrous
chlorobenzene (2 mL) was added via a syringe. The vial was heated in microwave reactor at
150 °C for 70 mins. The raw product was precipitated into methanol and collected by filtration.
The precipitate was then subjected to Soxhlet extractor and washed with methanol,
dichloromethane, and chloroform. The final polymers were obtained by precipitating in
acetone and drying in vacuum for 24 h, yielding PNTz4T (101 mg, 81%). GPC: Mn (63.7 Da),
Mw (132.4 Da), PDI (2.07).
SBr
NS
N
NS
NC12H25
C10H21
SBr
C12H25C10H21
S SMe3Sn
F
SnMe3+S
NS
N
NS
NC12H25
C10H21
S
C12H25C10H21
S S
Fn
Pd2(dba)3 2%,P(o-Tol)3 8%
MW: 120 oC 10 mins150 oC 70 mins
PNTz4T-1F
PNTz4T-1F: 5,10-Bis(5-bromo-4-(2-decyltetradecyl)thiophen-2-yl)naphtho[1,2-c:5,6-
c′]bis[1,2,5]thiadiazole (124 mg, 0.10 mmol) and 5,5’-bis(trimethylstannyl)-3-fluoro-2,2’-
bithiophene (51 mg, 0.10 mmol) were added into a 5 mL microwave tube. Pd2(dba)3 (1.8 mg,
2 μmol) and P(o-Tol)3 (2.4 mg, 8 μmol) were charged in the glove box. After capping,
anhydrous chlorobenzene (2 mL) was added via a syringe. The vial was heated in microwave
reactor at 150 °C for 70 mins. The raw product was precipitated into methanol and collected
by filtration. The precipitate was then subjected to Soxhlet extractor and washed with
methanol, dichloromethane, and chloroform. The final polymers were obtained by
precipitating in acetone and drying in vacuum for 24 h, yielding PNTz4T-1F (113 mg, 90%).
GPC: Mn (146.7 kDa), Mw (440.9 kDa), PDI (3.01).
SBr
NS
N
NS
NC12H25
C10H21
SBr
C12H25C10H21
S SMe3Sn
F
SnMe3+S
NS
N
NS
NC12H25
C10H21
S
C12H25C10H21
S S
Fn
Pd2(dba)3 2%,P(o-Tol)3 8%
MW: 120 oC 10 mins150 oC 70 mins
PNTz4T-2F
FF
PNTz4T-2F: 5,10-Bis(5-bromo-4-(2-decyltetradecyl)thiophen-2-yl)naphtho[1,2-c:5,6-
c′]bis[1,2,5]thiadiazole (124 mg, 0.10 mmol) and 5,5’-bis(trimethylstannyl)-3,3’-difluoro-2,2’-
bithiophene (53 mg, 0.10 mmol) were added into a 5 mL microwave tube. Pd2(dba)3 (1.8 mg,
2 μmol) and P(o-Tol)3 (2.4 mg, 8 μmol) were charged in the glove box. After capping,
anhydrous chlorobenzene (2 mL) was added via a syringe. The vial was heated in microwave
reactor at 150 °C for 70 mins. The raw product was precipitated into methanol and collected
by filtration. The precipitate was then subjected to Soxhlet extractor and washed with
methanol, dichloromethane, and chloroform. The final polymers were obtained by
precipitating in acetone and drying in vacuum for 24 h, yielding PNTz4T-2F (118 mg, 92%).
GPC: Mn (139.7 kDa), Mw (448.3 kDa), PDI (3.21).
Fig. S1 (a) Thermogravimetric analysis (TGA) (b) differential scanning calorimetry (DSC) and
(c) cyclic voltammetry (CV) of PNTz4T, PNTz4T-1F and PNTz4T-2F polymers.
Fig. S2 Torsional angle profiles of the (a) PNTz4T, (b) PNTz4T-1F and (c) PNTz4T-2F polymers
(for the simplicity of calculations, alkyl chain C10C12 of thiophene is replaced by methyl group
and two repeating units are used for geometric optimizations with B3LYP fine).
Table S1 Torsional angle profiles for the PNTz4T-based polymer series.
Polymer θ1o θ2
o θ3o θ4
o θ5o
PNTz4T 2.17 26.83 10.70 36.15 22.46
PNTz4T-1F 11.09 42.27 3.41 36.53 10.92
PNTz4T-2F 12.97 43.21 6.97 23.24 10.08
Fig. S3 (a) Current density-voltage (J-V) characteristics and (b) external quantum efficiency
(EQE) curves of o-xylene-processed PSCs with polymer:PC71BM films.
Table S2 Photovoltaic parameters of the o-xylene-processed PSCs with polymer:PC71BM films
under 1 sun illumination (AM 1.5G, 100 mW/cm2)
Polymerd
[nm]
VOC
[V]
JSC
[mA/cm2]
FF
[%]
PCE
[%]
~250 0.72 4.42 60 1.93
PNTz4T
~110 0.73 4.91 (4.87)a) 65 2.35
~270 0.78 3.76 54 1.60
PNTz4T-1F
~110 0.78 4.36 (4.35)a) 63 2.18
~250 0.84 3.06 52 1.37
PNTz4T-2F
~110 0.85 3.43 (3.41)a) 60 1.77
a)The value is calculated from EQE data.
Fig. S4 Graphical representation of statistical data obtained of (a) PNTz4T:PC71BM (b) PNTz4T-
1F:PC71BM and (c) PNTz4T-2F:PC71BM blend films with optimum conditions.
Table S3 Statistical results of (a) PNTz4T:PC71BM (b) PNTz4T-1F:PC71B and (c) PNTz4T-
2F:PC71BM blend films under optimal conditions.
Polymerd
[nm]
VOC
[V]
JSC
[mA/cm2]
FF
[%]
PCEa)
[%]
PNTz4T ~2500.73 ±
0.00
18.33 ±
0.1671 ± 0.75 9.60 ± 0.09
PNTz4T-1F ~2700.78 ±
0.00
20.42 ±
0.1571 ± 1.04
11.51 ±
0.14
PNTz4T-2F ~2500.81 ±
0.00
17.86 ±
0.3870 ± 1.47
10.33 ±
0.11
a)The average PCE is obtained from over 20 independent devices.
Fig. S5 Certified PCE of 11.67% obtained from Korea Institute of Energy Research (KIER) with
PNTz4T-1F:PC71BM blend film under optimum conditions.
Fig. S6 (a) Hole and (b) electron mobilities of polymer:PC71BM blends under optimized
conditions.
0.0 0.2 0.4 0.6 0.8
-18
-15
-12
-9
-6
-3
0
Curr
ent D
ensi
ty (m
A/cm
2 )
Voltage (V)
100 nm 150 nm 200 nm 250 nm 310 nm 390 nm
Fig. S7 J-V graphs of PNTz4T:PC71BM blend with different thicknesses under optimized device
conditions.
Table S4 Photovoltaic parameters of PNTz4T:PC71BM blend with different thicknesses under
optimized device conditions.
Polymer ThicknessVOC
[V]
JSC
[mA/cm2]
FF
[%]
PCE
[%]
100~ 0.737 11.768 72.93 6.33
150~ 0.745 15.144 72.59 8.20
200~ 0.746 16.361 72.29 8.83
250~ 0.736 18.19 72.70 9.73
300~ 0.722 18.13 70.22 9.20
PNTz4T
400~ 0.722 17.356 67.98 8.52
0.0 0.2 0.4 0.6 0.8-21-18-15-12-9-6-30
100 nm 160 nm 210 nm 270 nm 320 nm 410 nm
Curr
ent D
ensi
ty (m
A/cm
2 )
Voltage (V)
Fig. S8 J-V graphs of PNTz4T-1F:PC71BM blend with different thicknesses under optimized
device conditions.
Table S5 Photovoltaic parameters of PNTz4T-1F:PC71BM blend with different thicknesses
under optimized device conditions.
Polymer ThicknessVOC
[V]
JSC
[mA/cm2]
FF
[%]
PCE
[%]
100~ 0.778 13.619 74.43 7.89
150~ 0.785 17.943 74.11 10.44
200~ 0.787 18.832 74.03 10.98
270~ 0.789 20.378 73.14 11.77
350~ 0.773 19.758 71.97 11.00
PNTz4T-1F
400~ 0.786 19.33 67.66 10.28
0.0 0.2 0.4 0.6 0.8-18
-15
-12
-9
-6
-3
0 100 nm 150 nm 200 nm 250 nm 300 nm 390 nm
Curr
ent D
ensi
ty (m
A/cm
2 )
Voltage (V)
Fig. S9 J-V graphs of PNTz4T-2F:PC71BM blend with different thicknesses under optimized
device conditions.
Table S6 Photovoltaic parameters of PNTz4T-2F:PC71BM blend with different thicknesses
under optimized device conditions.
Polymer ThicknessVOC
[V]
JSC
[mA/cm2]
FF
[%]
PCE
[%]
100~ 0.803 11.990 72.52 6.98
150~ 0.813 13.994 72.87 8.29
200~ 0.813 16.537 72.04 9.69
250~ 0.819 17.904 71.62 10.50
300~ 0.811 17.195 68.02 9.48
PNTz4T-2F
400~ 0.807 16.690 63.45 8.55
Fig. S10 Series resistances measured from best J-V curves under area for (a) PNTz4T, (b)
PNTz4T-1F and (c) PNTz4T-2F polymers-based PSCs.
Fig. S11 Two dimensional GIWAXS images of (a) PNTz4T, (b) PNTz4T-1F and (c) PNTz4T-2F
neat polymer films processed from o-xylene solvent. (d) Out-of-plane (OOP) and (e) in-plane
(IP) line-cut profiles from GIWAXS patterns.
Table S7 Summary of the d-spacing parameters of edge-on and face-on orientation of neat
polymers.
Filma) (100)b) [Å] (010)b) [Å] (100)c) [Å] (010)c) [Å]
PNTz4T 23.74 - - -
PNTz4T-1F 19.82 - 21.71 3.56
PNTz4T-2F 22.18 - - 3.63
a)Films are processed from o-xylene; Calculation from b)OOP and c)IP direction.
Fig. S12 Two dimensional GIWAXS images of (a) PNTz4T:PC71BM, (b) PNTz4T-1F:PC71BM and
(c) PNTz4T-2F:PC71BM films processed from o-xylene solvent. (d) Out-of-plane (OOP) and (e)
in-plane (IP) line-cut profiles from GIWAXS patterns.
Table S8 Summary of the d-spacing parameters of edge-on and face-on orientation of
polymer:PC71BM from o-xylene solvent.
Filma) (100)(b) [Å] (010)b) [Å] (100)c) [Å] (010)c) [Å]
PNTz4T:PC71BM 22.68 - 24.31 3.67
PNTz4T-1F:PC71BM 19.70 3.50 21.39 3.59
PNTz4T-2F:PC71BM 21.53 3.48 23.57 3.56
a)Films are processed from o-xylene; Calculation from b)OOP and c)IP direction.
Fig. S13 NEXAFS TEY mode of (a) PNTz4T:PC71BM, (b) PNTz4T-1F:PC71BM and (c) PNTz4T-
2F:PC71BM blend films under optimum conditions at different incident angles.
Fig. S14 Contact angles of neat PC71BM and polymer:PC71BM blend films over ZnO NPs/PEIE
layer.
Table S9 Contact angles and surface energies of neat PC71BM and polymer:PC71BM blend
films.
Film
Deionized
Water
[θ]
Diiodomethane
[θ]
Surface
Energy
[mN/m]
ZnO NPs/PEIE/PC71BM 92.80 38.00 40.70[S8]
ZnO NPs/PEIE/PNTz4T 110.70 64.30 26.97
ZnO NPs/PEIE/PNTz4T-1F 112.00 63.30 27.89
ZnO NPs/PEIE/PNTz4T-2F 112.10 63.20 27.96
Contact angles were measured by Using “Drop Shape Analyzer, DSA 100” made by KRUSS,
Germany. Owen’s Method was employed to measure the surface energy by using drops from
two different liquids.
Fig. S15 Composition depth profiles of (a) PNTz4T:PC71BM, (b) PNTz4T-1F:PC71BM and (c)
PNTz4T-2F:PC71BM photoactive films by SIMS (positive mode).
Fig. S16 Composition depth profiles of (a) PNTz4T:PC71BM, (b) PNTz4T-1F:PC71BM and (c)
PNTz4T-2F:PC71BM photoactive films by SIMS (negative mode).
Table S10 Relative ratios of the polymer:PC71BM per unit area, calculated from the images
shown in Fig. 6.
Polymer Position [%] Acceptor [%]
Top 52.5 47.5
PNTz4T
Bottom 50.6 49.4
Top 52.5 47.5
PNTz4T-1F
Bottom 51.6 48.4
Top 61.8 38.2
PNTz4T2-2F
Bottom 62.8 37.2
Fig. S17 Cross-sectional TEM images of PSCs with (a) PNTz4T:PC71BM, (b) PNTz4T-1F:PC71BM
and (c) PNTz4T-2F:PC71BM photoactive films.
Fig. S18 Cross-sectional TEM image and EDS (S, Zn, Mo, Ag and In) mapping of
PNTz4T:PC71BM-based PSC.
Fig. S19 Cross-sectional TEM image and EDS (S, Zn, Mo, Ag and In) mapping of PNTz4T-
1F:PC71BM-based PSC.
Fig. S20 Cross-sectional TEM image and EDS (S, Zn, Mo, Ag and In) mapping of PNTz4T-
2F:PC71BM-based PSC.
Fig. S21 J-V curves of (a) PNTz4T:PC71BM, (b) PNTz4T-1F:PC71BM and (c) PNTz4T-2F:PC71BM-
based PSCs under optimized device conditions with respect to light intensity.
Polymer
Optical
Band-gap
[eV]
VOC
[V]
JSC
[mA/cm2]
FF
[%]
PCE
[%]Ref.
PDTP-DFBT 1.38 0.68 17.80 65 7.90 S3
C3-DPPTT-T 1.39 0.57 23.50 66 8.80 S4
PBDPP-TS 1.40 0.77 15.70 64 8.04 S5
PffBT4T-2OD 1.65 0.77 18.40 74 10.50 S6
PNT4T-2OD 1.56 0.76 19.80 68 10.10 S6
PffBT4T-C9C
13 1.66 0.784±0.004 19.8±0.4 73±111.3±0.1
(11.70)S7
PNTz4T-5MTC 1.56 0.73 18.07 72 9.66 S8
3F 1.57 0.82 15.70 71 9.14 S9
P4TNTz-2F 1.60 0.82 19.45 66 10.62 S10
PffBT-T3(1,2)-2 1.63 0.82 18.70 68 10.50 S11
P2 1.75 0.81 15.04 74 9.02 S12
PDTBTBz-2Fanti 1.90 0.97 14.00 72 9.80 S13
PDBT-T1 2.00 0.92 14.11 75 9.74 S14
PNTz4T-1F 1.59 0.78 ± 0.00 20.42±0.15 71±111.51±0.14
(11.77)
This
work
Table S11 PCEs reported in literature using polymer donors and PC71BM as acceptors in single
junction PSCs.
1.2 1.3 1.4 1.5 1.6 1.7 1.8 1.9 2.0 2.156789
101112 PNTz4T-1F
PCE
(%)
Optical Bandgap (eV)
Fig. S22 Plots of PCEs based on fullerene-based PSCs against optical bandgap.
Fig. S23 1H NMR of compound 6.
Fig. S24 1H NMR of compound 7.
Fig. S25 1H NMR of compound 8.
Fig. S26 13C NMR of compound 8.
References
S1 K. Kawashima, T. Fukuhara, Y. Suda, Y. Suzuki, T. Koganezawa, H. Yoshida, H. Ohkita, I.
Osaka, K. Takimiya, J. Am. Chem. Soc., 2016, 138, 10265.
S2 M. Wang, X. Hu, P. Liu, W. Li, X. Gong, F. Huang and Y. Cao, J. Am. Chem. Soc., 2011,
133, 9638.
S3 J. You, L. Dou, K. Yoshimura, T. Kato, K. Ohya, T. Moriarty, K. Emery, C.-C. Chen, J. Gao,
G. Li and Y. Yang, Nat. Commun., 2013, 4, 2411.
S4 R. S. Ashraf, I. Meager, M. Nikolka, M. Kirkus, M. Planells, B. C. Schroeder, S. Holliday,
M. Hurhangee, C. B. Nielsen, H. Sirringhaus and I. Mcculloch, J. Am. Chem. Soc., 2015,
137, 1314.
S5 L. Ye, X. Jiao, S. Zhang, H. Yao, Y. Qin, H. Ade and J. Hou, Adv. Energy Mater., 2016, 7,
1601138.
S6 Y. Liu, J. Zhao, Z. Li, C. Mu, W. Ma, H. Hu, K. Jiang, H. Lin, H. Ade and H. Yan, Nat.
Commun., 2014, 5, 5293.
S7 J. Zhao, Y. Li, G. Yang, K. Jiang, H. Lin, H. Ade, W. Ma and H. Yan, Nat. Energy,
2016, 1, 15027.
S8 S. Rasool, D. V. Vu, C. E. Song, H. K. Lee, S. K. Lee, J. C. Lee, S. J. Moon and W. S.
Shin, Adv. Energy Mater. 2019, 9, 1900168.
S9 J. W. Jo, J. W. Jung, E. H. Jung, H. Ahn, T. J. Shin and W. H. Jo, Energy Environ. Sci.,
2015, 8, 2427.
S10J. Lee, D. H. Sin, B. Moon, J. Shin, H. G. Kim, M. Kim and K. Cho, Energy Environ.
Sci., 2017, 10, 247.
S11H. Hu, K. Jiang, G. Yang, J. Liu, Z. Li, H. Lin, Y. Liu, J. Zhao, J. Zhang, F. Huang, Y.
Qu, W. Ma and H. Yan, J. Am. Chem. Soc., 2015, 137, 14149.
S12G. P. Kini, S. Oh, Z. Abbas, S. Rasool, M. Jahandar, C. E. Song, S. K. Lee, W. S. Shin,
W.-W. So and J.-C. Lee, ACS Appl. Mater. Interfaces, 2017, 9, 12617.
S13S.-J. Ko, Q. V. Hoang, C. E. Song, M. A. Uddin, E. Lim, S. Y. Park, B. H. Lee, S. Song,
S.-J. Moon, S. Hwang, P.-O. Morin, M. Leclerc, G. M. Su, M. L. Chabinyc, H. Y. Woo,
W. S. Shin and J. Y. Kim, Energy Environ. Sci., 2017, 10, 1443.
S14L. Huo, T. Liu, X. Sun, Y. Cai, A. J. Heeger and Y. Sun, Adv. Mater., 2015, 27, 2938.